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Polymer-supported monolayers

Lehmann T, Riihe J (1999) Polyethyloxazoline monolayers for polymer supported biomembrane models. Macromol Symp 142 1-12... [Pg.73]

This method is a combination of the other two methods. In our opinion, it is the most gentle method to reconstitute membrane proteins into supported bilayers and to prepare supported bilayers with fragile coexisting liquid phases of lipids. A LB monolayer is prepared on a hydrophilic substrate as described above. To prepare tethered-polymer supported bilayers, a suitable lipopolymer may be included at a concentration of a few... [Pg.2230]

There are various potential applications of photophysical phenomena in analytical chemistry. The relatively short lifetimes of most excited states, however, is a serious drawback to the construction of practical devices but studies which focus on finding ways to extend triplet lifetimes have now been described by Harriman et al. Kneas et al. have examined new types of luminescent sensor on polymer supports, and both Neurauter et al. and Marazuela et al. have designed sensors based on the ruthenium(II) polypyridine complex for the detection of carbon dioxide. A system, based on the formation of twisted intramolecular charge transfer states, has been devised for measuring the molecular weight of polymeric matrices (Al-Hassan et a/.), and the chemical reactivity at the interface of self-assembled monolayers has been assessed using fluorescence spectroscopy (Fox et al). [Pg.2]

Thus a-helical monolayers can be obtained from solvent I on the surface in this case, the stable conformation in the three-dimensional spreading phase is not modified by the interface (35, 36). Therefore the polymer-support interactions are not as great as the polymer-polymer interactions, as confirmed by the small variation of the first degree coefficient of the equations of the two-dimensional state with temperature (Table I). [Pg.362]

Other applications of photochemistry include the development of sensitive fluorescent chemosensors for analysis of dilute solutions of inorganic cations and anions and the study of the diffusion of individual molecules in solution at room temperature. Fluorescent compoimds have been used as replacements for radioisotopes in the analysis of biological compoimds and the study of biologically active compounds and living systems. Photochemical reactions also offer alternative probes for the characterization of the microenvironments in diverse solid and liquid media, including crystals, zeolites, alumina, silica and clay surfaces, semiconductor surfaces, liquid crystals and host-guest inclusion complexes, polymer films, monolayers and supported multilayers of surfactant molecules, mi-celles, and dendrimers. ... [Pg.859]

In this chapter we describe the basic principles involved in the controlled production and modification of two-dimensional protein crystals. These are synthesized in nature as the outermost cell surface layer (S-layer) of prokaryotic organisms and have been successfully applied as basic building blocks in a biomolecular construction kit. Most importantly, the constituent subunits of the S-layer lattices have the capability to recrystallize into iso-porous closed monolayers in suspension, at liquid-surface interfaces, on lipid films, on liposomes, and on solid supports (e.g., silicon wafers, metals, and polymers). The self-assembled monomolecular lattices have been utilized for the immobilization of functional biomolecules in an ordered fashion and for their controlled confinement in defined areas of nanometer dimension. Thus, S-layers fulfill key requirements for the development of new supramolecular materials and enable the design of a broad spectrum of nanoscale devices, as required in molecular nanotechnology, nanobiotechnology, and biomimetics [1-3]. [Pg.333]

Most important for many applications of S-layer lattices in molecular nanotechnology, biotechnology, and biomimetics was the observation that S-layer proteins are capable of reassembling into large coherent monolayers on solid supports (e.g., silicon wafers, polymers, metals) at the air/water interface and on Langmuir lipid films (Fig. 6) (see Sections V and VIII). [Pg.343]

An open-tubular column is a capillary bonded with a wall-supported stationary phase that can be a coated polymer, bonded molecular monolayer, or a synthesized porous layer network. The inner diameters of open-tubular CEC columns should be less than 25 pm that is less than the inner diameters of packed columns. The surface area of fused silica tubing is much less than that of porous packing materials. As a result, the phase ratio and, hence, the sample capacity for open-tubular columns are much less than those for packed columns. The small sample capacity makes it difficult to detect trace analytes. [Pg.451]

In the first monolayer of conjugated model material, a model molecular solid or a polymer adsorbate, assume that no chemistry (covalent bonding) occurs, since, in the absence of, for example, mechanical rupturing, the bonds at the surface of the molecular film are completely satisfied. This assumption is supported by the fact that, at least for condensed molecular solids, vapor-deposited films may be re-evaporated (removed) from the surface by gentle heating in UHV. [Pg.143]

Figure 3.9 illustrates the electrochemical and mass transport events that can occur at an electrode modified with a interfacial supramolecular assembly [9]. For monolayers in contact with a supporting electrolyte, the principal process is heterogeneous electron transfer across the electrode/monolayer interface. However, as discussed later in Chapter 5, thin films of polymers [10] represent an important class of interfacial supramolecular assembly (ISA) in which the properties of the redox center are affected by the physico-chemical properties of the polymer backbone. To address the properties of these thin films, mass transfer and reaction kinetics have to be considered. In this section, the properties of an ideally responding ISA are considered. [Pg.72]

Retention in supercritical chromatography is affected by the nature of both the mobile and the stationary phase. A variety of stationary phases, including high boiling liquids, polymer films, solid supports and chemically bonded monolayers, has been used. [Pg.102]


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Polymers monolayers

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